{"Abbreviation":["4-MeO-mor-T"],"Aliases":["Schembl24723279"],"ChemicalClasses":["morpholinylethylindole"],"Chirality":"achiral","Erowid Experience Reports":[],"Esters":[],"Formating":[],"HeavyAtomCount":19,"IUPACName":"4-[2-(4-methoxy-1H-indol-3-yl)ethyl]morpholine","InChI":"InChI=1S/C15H20N2O2/c1-18-14-4-2-3-13-15(14)12(11-16-13)5-6-17-7-9-19-10-8-17/h2-4,11,16H,5-10H2,1H3","InChIKey":"YNARZDNCYJBXSF-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e15\u003c/sub\u003eH\u003csub\u003e20\u003c/sub\u003eN\u003csub\u003e2\u003c/sub\u003eO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"260.33 g/mol","PubChemId":166106970,"PubChemTitle":"4-[2-(4-methoxy-1H-indol-3-yl)ethyl]morpholine","Reddit Experience Reports":[],"RefCount":2,"RefCur":"","References":[{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/166106970","Name":"4-Methoxy-N,N-morpholinyltryptamine","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 166106970, 4-Methoxy-N,N-morpholinyltryptamine. Accessed August 23, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/166106970\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/166106970\u003c/a\u003e"],"SMILES":"COC1=CC=CC2=C1C(=CN2)CCN3CCOCC3","SaltData":[],"Salts":[],"StereoisomerData":[],"Stereoisomers":[],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 113.705 68.956\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".8\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h114v69H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m31.807 1.063 3.344 10.392M33.704 18.631l-7.46 8.236\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m26.244 26.867-14.846-3.251M24.358 28.95l-12.107-2.651\"/\u003e\u003c/g\u003e\u003cpath d=\"M11.398 23.616 1.125 34.874\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M1.125 34.874 5.774 49.45M3.877 35.476l3.79 11.884\"/\u003e\u003c/g\u003e\u003cpath d=\"m5.774 49.45 14.914 3.175\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m20.688 52.625 10.273-11.257M19.829 49.949l8.374-9.177\"/\u003e\u003c/g\u003e\u003cpath d=\"m26.244 26.867 4.717 14.501M30.961 41.368l13.781 6.256\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m43.16 62.742 1.582-15.118M40.92 60.725l1.214-11.607\"/\u003e\u003c/g\u003e\u003cpath d=\"m43.16 62.742-11.412 2.42M20.688 52.625l5.374 9.382M44.742 47.624l13.224-7.575M57.966 40.049l13.172 7.664M71.138 47.713l9.943-5.695M84.377 36.038l.039-11.14M84.416 24.898l13.235-7.573M97.651 17.325l9.582 5.573M110.817 29.185l-.039 11.047M110.778 40.232l-13.235 7.573M87.639 42.044l9.904 5.761\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M36.478 13.526q-.738 0-1.173.554-.429.547-.429 1.494t.429 1.494q.435.548 1.173.548t1.167-.548q.428-.547.428-1.494t-.428-1.494q-.429-.554-1.167-.554m0-.548q1.053 0 1.679.709.631.702.631 1.887 0 1.179-.631 1.887-.626.703-1.679.703-1.054 0-1.685-.703-.631-.702-.631-1.887t.631-1.887q.631-.709 1.685-.709\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M26.397 63.395h.911l2.214 4.185v-4.185h.661v5.001h-.911l-2.22-4.185v4.185h-.655zM22.015 63.395h.679v2.048h2.459v-2.048h.672v5.001h-.672v-2.381h-2.459v2.381h-.679z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M82.469 37.638h.911l2.215 4.185v-4.185h.66v5h-.91l-2.221-4.185v4.185h-.655z\" class=\"atom\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M110.835 22.947q-.738 0-1.173.554-.428.548-.428 1.494 0 .947.428 1.494.435.548 1.173.548t1.167-.548q.429-.547.429-1.494 0-.946-.429-1.494-.429-.554-1.167-.554m0-.547q1.054 0 1.679.708.631.702.631 1.887 0 1.179-.631 1.887-.625.703-1.679.703-1.053 0-1.684-.703-.632-.702-.632-1.887t.632-1.887q.631-.708 1.684-.708\" class=\"atom\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m35.151 11.455-1.672-5.196M33.704 18.631l-3.73 4.118\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m31.748 65.162 5.706-1.21M26.062 62.007l-2.687-4.691M25.661 61.307l-2.286-3.991M81.081 42.018l-4.972 2.847M84.377 36.038l.02-5.57\" class=\"hi\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m107.233 22.898-4.791-2.787M110.817 29.185l-.02 5.524\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m87.639 42.044 4.952 2.88\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"4-Methoxy-N,N-morpholinyltryptamine","XLogP":1.9}
